Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • NGS group
    Member
    • Apr 2013
    • 28

    How to call the core genome of bacteria

    Hi everyone,

    I am trying to build a SNP tree from a set of bacterial genomes (the same species), and the first step is going to get the core genome. However, I did not find any detail workflow for that. Does anyone know some software or pipelines that can complete such task?

    Thank you very much!

    Victor
  • rhinoceros
    Senior Member
    • Apr 2013
    • 372

    #2
    You could look around NCBI's ftp. Maybe your species is already in the SNP DB? If not, you might have to do all-vs-all blasts and clustering (maybe OrthoMCL) to find out the shared genes. What you want might be possible with eutils too. Oh and there's this pipeline called HAL that might do what you want..
    Last edited by rhinoceros; 08-05-2013, 10:17 AM.
    savetherhino.org

    Comment

    • themerlin
      Member
      • Feb 2010
      • 51

      #3
      How many genomes are you working with? And are you working with assemblies or raw reads?

      For a smaller number of genome assemblies, you could do whole genome alignments with Mugsy (http://sourceforge.net/projects/mugsy/files/) or ProgressiveMauve (http://gel.ahabs.wisc.edu/mauve/), filter for blocks that are common to all genomes, then infer a phylogeny from the concatenated alignment? Is that what you had in mind?

      Jason

      Comment

      • NGS group
        Member
        • Apr 2013
        • 28

        #4
        Hi rhinoceros,

        Thank you for your reply. The aim of my project is to distinguish outbreak strains, so I have to do the analysis by myself. The HAL pipeline is what I want exactly. However I am not so familiar with commend line, is there any other more user-freindly pipeline or programs under Windows system?

        Victor
        Originally posted by rhinoceros View Post
        You could look around NCBI's ftp. Maybe your species is already in the SNP DB? If not, you might have to do all-vs-all blasts and clustering (maybe OrthoMCL) to find out the shared genes. What you want might be possible with eutils too. Oh and there's this pipeline called HAL that might do what you want..

        Comment

        • NGS group
          Member
          • Apr 2013
          • 28

          #5
          Hi Jason,

          Thank you for your reply. I am working with 15-20 genomes, which have been assembled. I am using Mauve now, but I think it is not easy to filter the common sequences by manual in Mauve. Do you mean that I just concatenate all common sequences by copy paste? Which alignment and phylogenetic tools are you going to use afterwards? Also Mauve?

          Victor

          Originally posted by themerlin View Post
          How many genomes are you working with? And are you working with assemblies or raw reads?

          For a smaller number of genome assemblies, you could do whole genome alignments with Mugsy (http://sourceforge.net/projects/mugsy/files/) or ProgressiveMauve (http://gel.ahabs.wisc.edu/mauve/), filter for blocks that are common to all genomes, then infer a phylogeny from the concatenated alignment? Is that what you had in mind?

          Jason

          Comment

          • themerlin
            Member
            • Feb 2010
            • 51

            #6
            Victor,

            If you have an aversion to command line tools, you could try this web server:



            You can upload assemblies, fastqs, vcfs, and/or bams and it will compute a tree. I haven't used it, but it might fit your needs.

            Jason

            Comment

            • NGS group
              Member
              • Apr 2013
              • 28

              #7
              This is a nice web tool. Thank you very much, Jason.

              Originally posted by themerlin View Post
              Victor,

              If you have an aversion to command line tools, you could try this web server:



              You can upload assemblies, fastqs, vcfs, and/or bams and it will compute a tree. I haven't used it, but it might fit your needs.

              Jason

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Cancer Drug Resistance: The Lingering Barrier to Rising Survival
                by SEQadmin2



                Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

                There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
                Today, 05:17 AM
              • GATTACAT
                Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                by GATTACAT
                Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
                07-01-2026, 11:43 AM
              • SEQadmin2
                Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                by SEQadmin2


                I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

                Here are nine questions we think about, in roughly the order they matter, before...
                06-18-2026, 07:11 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, Today, 10:08 AM
              0 responses
              6 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, Yesterday, 11:05 AM
              0 responses
              8 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-02-2026, 11:08 AM
              0 responses
              31 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 06-30-2026, 05:37 AM
              0 responses
              29 views
              0 reactions
              Last Post SEQadmin2  
              Working...